Grant: Discovery Grants Program - Individual
Concordia University
$65,000.00
Theoretical studies of molecular interactions, chemical reactions and spectroscopy
EF 2008-09
Résumé
With the recent advances in ultrafast spectroscopy, which now permit the observation of chemical reactions in real time, there is an ever increasing interest in theoretical studies of chemical reaction dynamics, as they can predict, explain and guide experiments. In particular, molecular dynamics techniques allow the motions of atoms and molecules to be simulated at the microscopic level, providing invaluable information about the mechanism and kinetics of chemical reactions. Dynamical studies are essential since they provide a link between potential energy surfaces calculated by electronic structure theory (quantum chemistry) and experimental measurements of chemical dynamics. In many instances, experimental observables are too convoluted to explain and understand without the help of theory. Furthermore, connection with experiment is crucial for assessing the reliability of computer simulations and theoretical models, which, in turn can be used to improve our fundamental understanding of chemistry.
New directions are proposed for the development of tools aimed at realistic computer simulations, which include an improved description of molecular interactions and the inclusion of quantum nuclear effects and possible nonadiabatic effects in dynamical simulations. Most applications will focus on clusters, which are aggregates of atoms or molecules which bridge the gap between the gas and condensed (liquid) phases. Clusters can be used as tools for selective microsolvation, or they can be a distinct class of materials with unique properties. We will study, in particular, 1) the fragmentation and reactions of cluster materials, 2) cluster and bulk microsolvation, 3) cluster photochemical processes and 4) probing molecular interactions and monitoring molecular dynamics with spectroscopy, in clusters, solution and complex environments. Our theoretical studies will help explain and guide experimental studies, and will contribute to a deeper molecular-level understanding of chemistry, with diverse potential applications from nanotechnology (e.g. hydrogen/energy storage) to biology (e.g. protein denaturation).
Programme
Discovery Grants Program - Individual
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
NSERC's Awards Data
Tel que publié
Application id
216940-2008
Name nom
Peslherbe, Gilles
Department département
Chemistry and Biochemistry
Organization id
70
Institution établissement
Concordia University
Province en
Québec
Province fr
Québec
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2008
Competition year année de concours
2008
Award amount
65000
Program id
RGPIN
Program nane en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
26
Committee name en
Anal. & Phys. Chemistry
Committee name fr
Chimie analytique et physique
Area of application code
1202
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Physical sciences
Area of application fr
Sciences physiques
Research subject code
3150
Research subject group en
Theoretical physics and chemistry
Research subject group fr
Physique et chimie théoriques
Research subject en
Theoretical physics and chemistry
Research subject fr
Physique et chimie théoriques
Partie
1
Nb partie
5
Application title
Theoretical studies of molecular interactions, chemical reactions and spectroscopy
Keyword
NA
Application summary
With the recent advances in ultrafast spectroscopy, which now permit the observation of chemical reactions in real time, there is an ever increasing interest in theoretical studies of chemical reaction dynamics, as they can predict, explain and guide experiments. In particular, molecular dynamics techniques allow the motions of atoms and molecules to be simulated at the microscopic level, providing invaluable information about the mechanism and kinetics of chemical reactions. Dynamical studies are essential since they provide a link between potential energy surfaces calculated by electronic structure theory (quantum chemistry) and experimental measurements of chemical dynamics. In many instances, experimental observables are too convoluted to explain and understand without the help of theory. Furthermore, connection with experiment is crucial for assessing the reliability of computer simulations and theoretical models, which, in turn can be used to improve our fundamental understanding of chemistry.
New directions are proposed for the development of tools aimed at realistic computer simulations, which include an improved description of molecular interactions and the inclusion of quantum nuclear effects and possible nonadiabatic effects in dynamical simulations. Most applications will focus on clusters, which are aggregates of atoms or molecules which bridge the gap between the gas and condensed (liquid) phases. Clusters can be used as tools for selective microsolvation, or they can be a distinct class of materials with unique properties. We will study, in particular, 1) the fragmentation and reactions of cluster materials, 2) cluster and bulk microsolvation, 3) cluster photochemical processes and 4) probing molecular interactions and monitoring molecular dynamics with spectroscopy, in clusters, solution and complex environments. Our theoretical studies will help explain and guide experimental studies, and will contribute to a deeper molecular-level understanding of chemistry, with diverse potential applications from nanotechnology (e.g. hydrogen/energy storage) to biology (e.g. protein denaturation).